copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.
<h4>Background</h4>Inherited factors predisposing individuals to breast and ovarian cancer are largely unidentified in a majority of families with hereditary breast and ovarian cancer (HBOC). We aimed to identify germline copy number variations (CNVs) contributing to HBOC susceptibility...
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| Auteurs principaux: | , , , , , |
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| Format: | article |
| Langue: | EN |
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Public Library of Science (PLoS)
2013
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| Accès en ligne: | https://doaj.org/article/4842ef037dbe436a9fc91a1bc1c7d1af |
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